Canonical Allele Identifier: CA2671693523

Gene: HADH

Linked Data

• gnomAD v4: 4-108027635-ATACC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.108027636_108027639del , CM000666.2:g.108027636_108027639del	GRCh38
NC_000004.11:g.108948792_108948795del , CM000666.1:g.108948792_108948795del	GRCh37
NC_000004.10:g.109168241_109168244del	NCBI36
NG_008156.2:g.42853_42856del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000507260.3:n.4795_4798del
ENST00000510728.6:n.1573_1576del
ENST00000514776.3:n.18_21del
ENST00000515462.7:n.1772_1775del
ENST00000626637.2:c.649-52_649-49del	ENSP00000486771.1:n.649-52_649-49del
ENST00000638648.2:c.649-52_649-49del	ENSP00000507949.1:n.649-52_649-49del
ENST00000640201.2:n.723-52_723-49del
ENST00000640752.2:n.4795_4798del
ENST00000682067.1:c.470-52_470-49del
ENST00000682086.1:n.654_657del
ENST00000682373.1:c.296-52_296-49del
ENST00000684696.1:c.637-303_637-300del	ENSP00000507675.1:n.637-303_637-300del
ENST00000309522.8:c.637-52_637-49del MANE Select	ENSP00000312288.4:n.637-52_637-49del
ENST00000403312.6:c.637-52_637-49del	ENSP00000385638.3:n.637-52_637-49del
ENST00000505878.4:c.814-52_814-49del	ENSP00000425952.2:n.814-52_814-49del
ENST00000514776.2:n.18_21del
ENST00000515462.6:n.1772_1775del
ENST00000638559.1:c.495-52_495-49del
ENST00000638621.1:c.223-52_223-49del	ENSP00000491581.1:n.223-52_223-49del
ENST00000638648.1:n.788-52_788-49del
ENST00000639146.1:c.637-52_637-49del	ENSP00000492345.1:n.637-52_637-49del
ENST00000639335.1:c.*72-52_*72-49del	ENSP00000491310.1:n.*72-52_*72-49del
ENST00000639698.1:c.516+4073_516+4076del	ENSP00000492420.1:n.516+4073_516+4076del
ENST00000639784.1:c.373+4073_373+4076del
ENST00000640048.1:c.609-52_609-49del	ENSP00000492009.1:n.609-52_609-49del
ENST00000640060.1:c.*732-52_*732-49del	ENSP00000492734.1:n.*732-52_*732-49del
ENST00000640201.1:n.592-52_592-49del
ENST00000640752.1:n.4788_4791del
ENST00000309522.7:c.637-52_637-49del	ENSP00000312288.3:n.637-52_637-49del
ENST00000403312.5:c.814-52_814-49del	ENSP00000385638.2:n.814-52_814-49del
ENST00000505878.3:c.649-52_649-49del	ENSP00000425952.1:n.649-52_649-49del
ENST00000507260.1:n.337-52_337-49del
ENST00000510728.5:n.125_128del
ENST00000603302.5:c.637-52_637-49del	ENSP00000474560.1:n.637-52_637-49del
ENST00000626637.1:c.649-52_649-49del	ENSP00000486771.1:n.649-52_649-49del
NM_001184705.2:c.637-52_637-49del	NP_001171634.2:n.637-52_637-49del
NM_005327.4:c.637-52_637-49del	NP_005318.3:n.637-52_637-49del
XM_005262972.1:c.649-52_649-49del	XP_005263029.1:n.649-52_649-49del
XR_938726.1:n.786-52_786-49del
NM_001331027.1:c.649-52_649-49del	NP_001317956.1:n.649-52_649-49del
XR_001741214.2:n.731-52_731-49del
XR_002959727.1:n.731-52_731-49del
NM_001184705.3:c.637-52_637-49del	NP_001171634.2:n.637-52_637-49del
NM_005327.7:c.637-52_637-49del MANE Select	NP_005318.6:n.637-52_637-49del
NM_001184705.4:c.637-52_637-49del	NP_001171634.3:n.637-52_637-49del
NM_001331027.2:c.649-52_649-49del	NP_001317956.2:n.649-52_649-49del